eudamed_udi
Primary ID: 05059441001096
CITADEL PLUS (UDI 05059441001096)
Manufactured by ArjoHuntleigh AB
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CITADEL PLUS - Primary ID 05059441001096
Device Regulatory Overview
The CITADEL PLUS (Model/Catalog Number: FXX21A4C4AKJBB) is a medical device manufactured by ArjoHuntleigh AB. This product is indexed under FDA Product Code / Category Classification V08060105 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- FXX21A4C4AKJBB
- Product Code / EMDN
- V08060105
- Device Name
- ENTERPRISE 9000X
- Database Sync Date
- 2026-08-09 16:28:56
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of CITADEL PLUS?
The registered manufacturer of record for CITADEL PLUS is ArjoHuntleigh AB.
What is the Primary UDI-DI identifier for CITADEL PLUS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05059441001096.
What classification code is assigned to this device?
This device is registered under product classification code V08060105.
Similar Classification Devices (V08060105)
Other Devices by ArjoHuntleigh AB
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